Canonical Allele Identifier: CA1683354010
Gene: GNA12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2830385_2830386delinsTC , CM000669.2:g.2830385_2830386delinsTC GRCh38
NC_000007.13:g.2870019_2870020delinsTC , CM000669.1:g.2870019_2870020delinsTC GRCh37
NC_000007.12:g.2836545_2836546delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275364.8:c.309+13467_309+13468delinsGA MANE Select ENSP00000275364.3:n.309+13467_309+13468de...
ENST00000275364.7:c.309+13467_309+13468delinsGA ENSP00000275364.3:n.309+13467_309+13468de...
NM_001293092.1:c.309+13467_309+13468delinsGA NP_001280021.1:n.309+13467_309+13468delin...
NM_007353.2:c.309+13467_309+13468delinsGA NP_031379.2:n.309+13467_309+13468delinsGA...
XM_011515288.1:c.19-35243_19-35242delinsGA XP_011513590.1:n.19-35243_19-35242delinsG...
XM_011515288.3:c.19-35243_19-35242delinsGA XP_011513590.1:n.19-35243_19-35242delinsG...
NM_007353.3:c.309+13467_309+13468delinsGA MANE Select NP_031379.2:n.309+13467_309+13468delinsGA...
NM_001293092.2:c.309+13467_309+13468delinsGA NP_001280021.1:n.309+13467_309+13468delin...
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